Comprehensive clinicopathological, molecular, and methylation analysis of mesenchymal tumors with NTRK and other kinase gene aberrations

IF 5.6 2区 医学 Q1 ONCOLOGY The Journal of Pathology Pub Date : 2024-02-09 DOI:10.1002/path.6260
Natálie Klubíčková, Josephine K Dermawan, Elaheh Mosaieby, Petr Martínek, Tomáš Vaněček, Veronika Hájková, Nikola Ptáková, Petr Grossmann, Petr Šteiner, Marián Švajdler, Zdeněk Kinkor, Květoslava Michalová, Peter Szepe, Lukáš Plank, Stanislava Hederová, Alexandra Kolenová, Neofit Juriev Spasov, Kemal Kosemehmetoglu, Leo Pažanin, Zuzana Špůrková, Martin Baník, Luděk Baumruk, Anders Meyer, Antonina Kalmykova, Olena Koshyk, Michal Michal, Michael Michal
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Abstract

Alterations in kinase genes such as NTRK1/2/3, RET, and BRAF underlie infantile fibrosarcoma (IFS), the emerging entity ‘NTRK-rearranged spindle cell neoplasms’ included in the latest WHO classification, and a growing set of tumors with overlapping clinical and pathological features. In this study, we conducted a comprehensive clinicopathological and molecular analysis of 22 cases of IFS and other kinase gene-altered spindle cell neoplasms affecting both pediatric and adult patients. Follow-up periods for 16 patients ranged in length from 10 to 130 months (mean 38 months). Six patients were treated with targeted therapy, achieving a partial or complete response in five cases. Overall, three cases recurred and one metastasized. Eight patients were free of disease, five were alive with disease, and two patients died. All cases showed previously reported morphological patterns. Based on the cellularity and level of atypia, cases were divided into three morphological grade groups. S100 protein and CD34 were at least focally positive in 12/22 and 14/22 cases, respectively. Novel PWWP2A::RET, NUMA1::RET, ITSN1::RAF1, and CAPZA2::MET fusions, which we report herein in mesenchymal tumors for the first time, were detected by RNA sequencing. Additionally, the first uterine case with BRAF and EGFR mutations and CD34 and S100 co-expression is described. DNA sequencing performed in 13 cases uncovered very rare additional genetic aberrations. The CNV profiles showed that high-grade tumors demonstrate a significantly higher percentage of copy number gains and losses across the genome compared with low- and intermediate-grade tumors. Unsupervised clustering of the tumors’ methylation profiles revealed that in 8/9 cases, the methylation profiles clustered with the IFS methylation class, irrespective of their clinicopathological or molecular features. © 2024 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

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对存在 NTRK 和其他激酶基因畸变的间质肿瘤进行全面的临床病理、分子和甲基化分析。
NTRK1/2/3、RET和BRAF等激酶基因的改变是婴儿纤维肉瘤(IFS)的病因,也是最新WHO分类中新出现的 "NTRK重组纺锤形细胞肿瘤 "的病因,同时也是越来越多临床和病理特征重叠的肿瘤的病因。在这项研究中,我们对 22 例 IFS 和其他激酶基因改变的纺锤形细胞肿瘤进行了全面的临床病理和分子分析,这些肿瘤既有儿童患者,也有成人患者。16 名患者的随访时间从 10 个月到 130 个月不等(平均 38 个月)。六名患者接受了靶向治疗,其中五例获得了部分或完全应答。总体而言,3 例复发,1 例转移。八名患者痊愈,五名患者带病生存,两名患者死亡。所有病例都显示出之前报道过的形态学模式。根据细胞度和不典型程度,病例被分为三个形态学等级组。分别有 12/22 例和 14/22 例患者的 S100 蛋白和 CD34 至少呈病灶阳性。通过 RNA 测序,我们首次在间质瘤中发现了 PWWP2A::RET、NUMA1::RET、ITSN1::RAF1 和 CAPZA2::MET 融合。此外,本文还描述了首例BRAF和表皮生长因子受体(EGFR)突变以及CD34和S100共表达的子宫癌病例。对13个病例进行的DNA测序发现了非常罕见的额外基因畸变。CNV图谱显示,与中低级别肿瘤相比,高级别肿瘤在整个基因组中拷贝数增减的比例明显更高。对肿瘤甲基化图谱的无监督聚类显示,在8/9个病例中,甲基化图谱与IFS甲基化类别聚类,而与临床病理或分子特征无关。© 2024 作者。病理学杂志》由约翰威利父子有限公司代表大不列颠及爱尔兰病理学会出版。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
The Journal of Pathology
The Journal of Pathology 医学-病理学
CiteScore
14.10
自引率
1.40%
发文量
144
审稿时长
3-8 weeks
期刊介绍: The Journal of Pathology aims to serve as a translational bridge between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The main interests of the Journal lie in publishing studies that further our understanding the pathophysiological and pathogenetic mechanisms of human disease. The Journal of Pathology welcomes investigative studies on human tissues, in vitro and in vivo experimental studies, and investigations based on animal models with a clear relevance to human disease, including transgenic systems. As well as original research papers, the Journal seeks to provide rapid publication in a variety of other formats, including editorials, review articles, commentaries and perspectives and other features, both contributed and solicited.
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